Clinical, neuroimaging and genetic profiles of amyotrophic lateral sclerosis with frontotemporal lobe degeneration
10.3760/cma.j.issn.1006-7876.2016.02.003
- VernacularTitle:肌萎缩侧索硬化合并额颞叶变性的临床、影像与遗传学特点
- Author:
Bo CUI
;
Liying CUI
;
Jing GAO
;
Na NIU
;
Yicheng ZHU
;
Caiyan LIU
;
Jing YUAN
;
Qing LIU
;
Zhen QIAO
;
Fang LI
;
Bo HOU
;
Feng FENG
- Publication Type:Journal Article
- Keywords:
Amyotrophic lateral sclerosis;
Frontotemporal lobar degeneration;
Electromyography;
Neuroimaging;
Cytogenetic analysis
- From:
Chinese Journal of Neurology
2016;(2):87-92
- CountryChina
- Language:Chinese
-
Abstract:
Objective To describe the clinical, neuroimaging and genetic profiles of amyotrophic lateral sclerosis with frontotemporal lobe degeneration ( ALS-FTLD).Methods From August 2011 to May 2015, patients with FTLD or other types of neurodegenerative dementia were physically examined in detail and electromyography was performed to those with suspected dysarthria, limb atrophy or weakness.Cognitive and behavioral screenings were performed to all ALS patients.Patients with ALS-FTLD entered further analysis of neuroimaging and genetics.Results Among the 8 patients diagnosed as ALS-FTLD, 4 patients began with personality change or amnesia, while diseases in the remaining 4 cases began with limb weakness or dysarthria.Dementia type of 7 cases was behavioral variant FTLD ( bvFTD) and 1 case was diagnosed as semantic dementia.Electromyography of all the 8 patients showed diffuse neurogenic changes.Constructional neuroimaging of 6 patients showed cerebral atrophy predominantly in frontal and temporal lobes.Fluorodeoxyglucose-positron emission tomography was conducted in 5 patients, indicating hypometabolism mainly in frontal and ( or) temporal lobes.NeuroQ analysis revealed that bilateral frontal lobes were the most hypometabolic areas for ALS-FTLD.Among 4 patients who underwent genetic screening, 1 patient was C9ORF72 mutation carrier.Conclusions bvFTD is the major type of dementia in the context of ALS.Metabolic neuroimaging could assist accurate diagnosis, and it reveals that bilateral frontal lobes are the most hypometabolic areas for ALS-FTLD.C9ORF72 gene mutation is an important pathogenic mutation for ALS-FTLD, although it is rare in Chinese population.
